Four New Cyclohexylideneacetonitrile Derivatives from the Hypocotyl of Mangrove (Bruguiera gymnorrhiza)
- Molecules. 2015 Aug 12;20(8):14565-75. doi: 10.3390/molecules200814565.
- 1. School of Pharmaceutical Sciences, Guangxi University of Chinese Medicine, Nanning 530001, China. [email protected].
- 2. School of Pharmaceutical Sciences, Guangxi University of Chinese Medicine, Nanning 530001, China. [email protected].
- 3. Guangxi Key Laboratory of Marine Environmental Science, Guangxi Academy of Sciences, Nanning 530007, China. [email protected].
- 4. School of Pharmaceutical Sciences, Guangxi University of Chinese Medicine, Nanning 530001, China. [email protected].
- 5. Guangxi Key Laboratory of Marine Environmental Science, Guangxi Academy of Sciences, Nanning 530007, China. [email protected].
- 6. School of Pharmaceutical Sciences, Guangxi University of Chinese Medicine, Nanning 530001, China. [email protected].
- 7. School of Pharmaceutical Sciences, Guangxi University of Chinese Medicine, Nanning 530001, China. [email protected].
- 8. School of Pharmaceutical Sciences, Guangxi University of Chinese Medicine, Nanning 530001, China. [email protected].
- 9. School of Pharmaceutical Sciences, Guangxi University of Chinese Medicine, Nanning 530001, China. [email protected].
- 10. School of Pharmaceutical Sciences, Guangxi University of Chinese Medicine, Nanning 530001, China. [email protected].
- 11. Key Laboratory of Plant Resources Conservation and Sustainable Utilization, South China Botanical Garden, Chinese Academy of Sciences, Guangzhou 510650, China. [email protected].
- 12. Guangdong Provincial Key Laboratory of Applied Botany, South China Botanical Garden, Chinese Academy of Sciences, Guangzhou 510650, China. [email protected].
Four new cyclohexylideneacetonitrile derivatives 1-4, named menisdaurins B-E, as well as three known cyclohexylideneacetonitrile derivatives--menisdaurin (5), coclauril (6), and menisdaurilide (7)--were isolated from the hypocotyl of a mangrove (Bruguiera gymnorrhiza). The structures of the isolates were elucidated on the basis of extensive spectroscopic analysis. Compounds 1-7 showed anti-Hepatitis B virus (HBV) activities, with EC50 values ranging from 5.1 ± 0.2 μg/mL to 87.7 ± 5.8 μg/mL.